Abstract

The Cre-Lox system is a highly versatile and powerful DNA recombinase mechanism, mainly used in genetic engineering to insert or remove desired DNA sequences. It is widely utilized across multiple fields of biology, with applications ranging from plants, to mammals, to microbes. A key feature of this system is its ability to allow recombination between mutant lox sites. Two of the most commonly used mutant sites are named lox66 and lox71, which recombine to create a functionally inactive double mutant lox72 site. However, a large portion of the published literature has incorrectly annotated these mutant lox sites, which in turn can lead to difficulties in replication of methods, design of proper vectors and confusion over the proper nomenclature. Here, we demonstrate common errors in annotations, the impacts they can have on experimental viability, and a standardized naming convention. We also show an example of how this incorrect annotation can induce toxic effects in bacteria that lack optimal DNA repair systems, exemplified by Mycoplasma pneumoniae .

Highlights

  • The Cre-­Lox system was first characterized in 1981 by Nat Sternberg and Daniel Harrison [1]

  • The first, the Cre recombinase, is a 38 kDa monomeric tyrosine recombinase. This protein acts upon a pair of 34 bp lox sites [locus of (x)crossing over], which consist of an 8 bp central spacer region flanked by two 13 bp inverted repeat regions [2, 3]

  • We show a comprehensive analysis of the literature associated with lox66 and lox71 sites, with examples of the common errors that have occurred in the nomenclature and a standardized naming convention to help resolve these remaining ambiguities

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Summary

Introduction

The Cre-­Lox system was first characterized in 1981 by Nat Sternberg and Daniel Harrison [1]. It is a DNA recombinase system derived from the P1 bacteriophage, and consists of two components. The first, the Cre recombinase, is a 38 kDa monomeric tyrosine recombinase. This protein acts upon a pair of 34 bp lox sites [locus of (x)crossing over], which consist of an 8 bp central spacer region flanked by two 13 bp inverted repeat regions [2, 3]. If the lox sites are in opposite (trans) orientations, the DNA between them is inverted as a consequence of the recombination event

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